SCHEMBL2151966

SCHEMBL2151966

Nc1ccc(C(=O)CBr)cc1

nearest known ligand 0.64

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
GSK3B P49841 11/20 0.64
PTPN1 P18031 6/20 0.64
LMNA P02545 2/20 0.45
CYP1A2 P05177 1/20 0.45
CYP3A4 P08684 1/20 0.45
MAOA P21397 1/20 0.45
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
CYP19A1 P11511 1/20 0.44
KDM4E B2RXH2 1/20 0.44
MAPT P10636 1/20 0.44
HIF1A Q16665 1/20 0.44
SLC22A6 Q4U2R8 1/20 0.44
SLC22A8 Q8TCC7 1/20 0.44
POLB P06746 1/20 0.43
PKM P14618 1/20 0.43
APEX1 P27695 1/20 0.43
TDP1 Q9NUW8 1/20 0.43

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL205280 0.87 GSK3B (0.80) GSK3BPTPN1
SCHEMBL3379031 0.81 GSK3B (0.64) GSK3BPTPN1CYP3A4KMT2AMAPT
SCHEMBL689331 0.80 GSK3B (0.83) GSK3BPTPN1LMNACYP1A2KDM4E
SCHEMBL28594745 0.80 GSK3B (0.70) GSK3BPTPN1LMNAMAPTPKM
SCHEMBL11365527 0.80 MAPT (0.56) PTPN1LMNACYP1A2CYP3A4MAOA
SCHEMBL1311272 0.79 L3MBTL1 (0.50) LMNAMAPTTDP1
SCHEMBL3373429 0.78 LMNA (0.47) LMNACYP1A2CYP3A4MAOAMEN1
SCHEMBL70930 0.78 GSK3B (1.00) GSK3BPTPN1
SCHEMBL9547546 0.78 LMNA (0.47) GSK3BLMNACYP1A2CYP3A4MAOA
SCHEMBL3181886 0.78 LMNA (0.47) LMNACYP1A2CYP3A4MAOAMEN1

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 51 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108383830-B Acridone stable isotope sulfhydryl compound marking reagent and synthesis method and application thereof 曲阜师范大学 2020-01-10 CN claimed
US-8354444-B2 Substituted pyrrolidine-2-carboxamides HOFFMANN-LA ROCHE INC. (US) 2013-01-15 US claimed
EP-2340021-B1 SUBSTITUTED PYRROLIDINE-2-CARBOXAMIDES HOFFMANN LA ROCHE (CH) 2012-11-07 EP claimed
US-20100152190-A1 Substituted Pyrrolidine-2-Carboxamides F. HOFFMANN-LA ROCHE AG (CH) 2010-06-17 US claimed
WO-2010031713-A1 SUBSTITUTED PYRROLIDINE-2-CARBOXAMIDES F. HOFFMANN-LA ROCHE AG (CH) 2010-03-25 WO claimed
US-20100075948-A1 Substituted Pyrrolidine-2-Carboxamides DING QINGJIE 2010-03-25 US claimed
WO-2026090173-A1 MODIFIED SELF-IMMOLATING MOIETIES IN ANTIBODY-DRUG CONJUGATES CODEABLE THERAPEUTICS, INCORPORATED (US) 2026-04-30 WO disclosed
US-20260070898-A1 PROCESS FOR THE PREPARATION OF FURAZANOBENZIMIDAZOLES AND CRYSTALLINE FORMS THEREOF GLIOBLASTOMA FOUND INC (US) 2026-03-12 US disclosed
US-20240352007-A1 PROCESSES FOR THE PREPARATION OF FURAZANOBENZIMIDAZOLES AND CRYSTALLINE FORMS THEREOF BASILEA PHARMACEUTICA INTERNATIONAL LTD, ALLSCHWIL (CH) 2024-10-24 US disclosed
EP-3615529-B1 PROCESSES FOR THE PREPARATION OF FURAZANOBENZIMIDAZOLES AND CRYSTALLINE FORMS THEREOF BASILEA PHARMACEUTICA INT AG ALLSCHWIL (CH) 2024-06-05 EP disclosed
US-11891382-B2 Processes for the preparation of furazanobenzimidazoles and crystalline forms thereof Basilea Pharmaceutica International AG 2024-02-06 US disclosed
CN-116947836-A Method for preparing furazanobenzimidazole and crystal forms thereof 巴斯利尔药物国际股份公司 2023-10-27 CN disclosed
CN-110536890-B Method for preparing furazanobenzimidazole and crystal forms thereof 巴斯利尔药物国际股份公司 2023-08-15 CN disclosed
WO-2007067993-A1 INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2007-06-14 WO disclosed
WO-2007067994-A1 INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2007-06-14 WO disclosed
US-20070065841-A1 Methods and compositions for the removal of nucleic acid amplification inhibitors ENERGY, U.S. DEPARTMENT OF 2007-03-22 US disclosed
US-20060030543-A1 Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease KALYPSYS, INC. 2006-02-09 US disclosed
WO-2005123089-A2 MULTICYCLIC SULFONAMIDE COMPOUNDS AS INHIBITORS OF HISTONE DEACETYLASE FOR THE TREATMENT OF DISEASE KALYPSYS, INC. (US) 2005-12-29 WO disclosed
US-4716169-A INOTROPIC AGENTS DR. KARL THOMAE GMBH (DE) 1987-12-29 US disclosed
EP-0185345-A1 Imidazo derivatives, their preparation and medicines containing them Dr. Karl Thomae GmbH (DE) 1986-06-25 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (7 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20060030543-A1 Multicyclic sulfonamide compounds as inhibitors of histone deacetylase for the treatment of disease HDAC6, HDAC3, HDAC5 GSK3B 153/4885PTPN1 2749/4885LMNA 1450/4885
US-11891382-B2 Processes for the preparation of furazanobenzimidazoles and crystalline forms thereof FANCI, CYP2F1, CYP4F3 GSK3B 2920/4885PTPN1 2720/4885LMNA 2122/4885
US-20100152190-A1 Substituted Pyrrolidine-2-Carboxamides ARG2, CCNY, PYCR1 GSK3B 4011/4885PTPN1 3496/4885LMNA 3002/4885
US-20240352007-A1 PROCESSES FOR THE PREPARATION OF FURAZANOBENZIMIDAZOLES AND CRYSTALLINE FORMS THEREOF FANCI, FANCD2, CYP2F1 GSK3B 2890/4885PTPN1 1875/4885LMNA 2020/4885
US-20260070898-A1 PROCESS FOR THE PREPARATION OF FURAZANOBENZIMIDAZOLES AND CRYSTALLINE FORMS THEREOF BRCA1, PRKDC, KIT GSK3B 946/4885PTPN1 1653/4885LMNA 143/4885
US-20070065841-A1 Methods and compositions for the removal of nucleic acid amplification inhibitors POLRMT, FBL, POLL GSK3B 3452/4885PTPN1 3866/4885LMNA 548/4885
US-20100075948-A1 Substituted Pyrrolidine-2-Carboxamides ARG2, CCNY, PYCR1 GSK3B 4011/4885PTPN1 3496/4885LMNA 3002/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.